So in summary, when we tested this in tumors, this looks very good, but we’ve also looked at different other organs. We’ve looked at intramuscular, intradermal, and also not just MC38 tumors but also Tc1 tumors. And you can see that we are having a full increase in delivery compared to just giving modified mRNA directly and also, specifically, as measured with the MC38 tumors versus LNPs. So for intratumoral immunotherapy, what you can do when you deliver is locally, you can have a systemic therapeutic effect that also can be achieved through immunomodulation depending on what you are delivering, such as like antigens or immunostimulating factors.
(Fra sist Q)